What is life like with DiGeorge syndrome?

What is life like with DiGeorge syndrome?

DiGeorge syndrome is a condition present from birth that can cause a range of lifelong problems, including heart defects and learning difficulties. The severity of the condition varies. Some children can be severely ill and very occasionally may die from it, but many others may grow up without realising they have it.

Is 22q the same as DiGeorge syndrome?

DiGeorge syndrome, more accurately known by a broader term — 22q11. 2 deletion syndrome — is a disorder caused when a small part of chromosome 22 is missing. This deletion results in the poor development of several body systems.

Is 22q deletion syndrome a disability?

Many children with 22q11. 2 deletion syndrome have developmental delays, including delayed growth and speech development, and some have mild intellectual disability or learning disabilities. Older affected individuals have difficulty reading, performing tasks involving math, and problem solving.

Can a child with 22q Deletion syndrome (DiGeorge syndrome) (VCFS) have high thyroid levels?

Thyroid levels can be too high or too low in children with 22q deletion syndrome (DiGeorge syndrome, VCFS). How is 22q Deletion Syndrome (DiGeorge Syndrome, VCFS) diagnosed?

What are the signs and symptoms of 22q Deletion syndrome (DiGeorge syndrome)?

Speech and feeding – Patients with 22q deletion syndrome (DiGeorge syndrome, VCFS) may have a cleft palate or poor function of the palate resulting in speech differences, delayed speech and difficulty feeding and swallowing.

How can I Help my Child with 22q Deletion Syndrome?

Early childhood intervention, speech, occupational therapy and physical therapies can be very helpful. Neurocognitive evaluation as children get older and in school can assist parents and teachers by providing recommendations for clinical management and academic support in the future. Where can I find a 22q deletion syndrome support group?

What is DiGeorge syndrome?

DiGeorge syndrome, more accurately known by a broader term — 22q11.2 deletion syndrome — is a disorder caused when a small part of chromosome 22 is missing. This deletion results in the poor development of several body systems. The term 22q11.2 deletion syndrome covers terms once thought to be separate conditions, including DiGeorge syndrome,